A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347298



Internal ID21004851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:183927938..184179691hg38UCSC Ensembl
chr2:184792665..185044418hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38251754
hg19251754
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205331
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347298
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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